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Arsenic is classified as one of the most toxic elements for humans by the World Health Organization (WHO). With the tightening drinking water regulation to 10 μg L −1 by the WHO, it is necessary to find efficient sorbent materials for arsenic. In this work, the removal of arsenic(V) from water is achieved with an insoluble chitosan sorbent in the protonated form obtained by a simple heating process. Kinetic studies show a very fast sorption (less than 10 min). The Langmuir isotherm model is best describing experimental data with a capacity of 42 mg g −1 at pH 8. The sorption process is based on anion exchange (chemisorption) determined from the Dubinin-Radushkevich model. The sorption efficiency of the chitosan sorbent is 97 % at low concentrations (e.g. 100 μg L −1). Thermodynamic analysis reveals that the sorption process is exothermic and is controlled by enthalpic factors. Breakthrough curves (BTC) were acquired in real-time by instrumental chromatography and was better described by the Thomas model. BTC from column sorption and desorption with a salt solution suggest that this sorbent is relevant for large scale applications. With this new renewable product, it will be possible to treat arsenic contaminated water at low cost and with little waste (concentration factor of 1500).

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BackgroundEngineered nanoparticles have unique properties compared to bulk materials and their commercial uses growing rapidly. They represent a potential risk for environment and health and could be eventually released in water. Silver nanoparticles (Ag NP) are applied in various products and are well-known for their antibacterial properties. Nowadays, pre-concentration and separation methods for Ag NP possess some limitations. Here, we present a simple, green method to sequestrate and concentrate Ag NP from different aqueous media.ResultsSupported polysaccharides on glass beads synthesized in water by a single step reaction show high sequestration capacity of citrate-coated Ag NP in aqueous media. Supported polysaccharides were characterized by infrared spectroscopy, scanning electron microscopy (SEM) and elemental analysis. Sequestration of 83.0 % of Ag NP was attained from a 20 μg.L−1 aqueous solution with supported chitosan in water whereas supported 2-hydroxyethylcellulose (HEC) reached 64.0 % in synthetic seawater in 2 h. The influence of polymer/glass beads ratio and molecular weight of polysaccharides was also studied. The effect of the salinity and humic acids on sequestration of Ag NP was investigated. Supported polymers have shown high performance for sequestration of ionic silver. Sequestration of 82.5 % and 80.8 % were obtained from a 60 μg.L−1 silver ion (as nitrate salt) with supported HEC and chitosan, respectively. Sequestrated Ag NP was characterized with transmission electron microscopy (TEM) where images showed Ag NP with unchanged size and shape.ConclusionsThis sequestration method, involving green synthesis, allows efficient concentration and characterization of Ag NP from different aqueous media. This simple and fast method is a potential sustainable technique for elimination of Ag NP and ionic silver from waste waters and waters at different salinities.